Potassium Chloride Tablets

FDA 510(k) K840843 · Bionostics, Inc.

Substantially Equivalent

510(k) numberK840843

Submission

Device name
Potassium Chloride Tablets
Applicant
Bionostics, Inc.
Walker, MI, US
Received
February 24, 1984
Decision date
April 17, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CHL – Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1120
Specialty
Clinical Chemistry

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Questions and answers

When was Potassium Chloride Tablets cleared by the FDA?

Potassium Chloride Tablets (K840843) received a 510(k) decision of Substantially Equivalent on April 17, 1984, 53 days after the submission was received.

What is the product code of K840843?

The FDA product code is CHL – Electrode Measurement, Blood-Gases (Pco2, Po2) And Blood Ph, a Class II (moderate risk) device regulated under 21 CFR 862.1120.